TY - JOUR
T1 - Bactericidal activity response of blood neutrophils from critically ill patients to in vitro granulocyte colony-stimulating factor stimulation
AU - Yang, Kun
AU - Azoulay, Élie
AU - Attalah, Lynda
AU - Zahar, Jean Ralph
AU - Van De Louw, Andry
AU - Cerf, Charles
AU - Soussy, Claude James
AU - Duvaldestin, Philippe
AU - Brochard, Laurent
AU - Brun-Buisson, Christian
AU - Harf, Alain
AU - Delclaux, Christophe
N1 - Funding Information:
This study was supported by a grant from Aventis France
PY - 2003/3/1
Y1 - 2003/3/1
N2 - Objective: Neutrophil function impairment is common in non-neutropenic critically ill patients. Whether granulocyte colony-stimulating factor (G-CSF) may be useful for preventing nosocomial infection in these patients is debated. The response of blood neutrophils from critically ill patients to G-CSF was investigated in vitro. Design and setting: Prospective study, laboratory investigation in two intensive care units. Patients: 52 critically ill patients without immunosuppression. Measurements: Neutrophils obtained from 52 patients on the 5th day of their intensive care unit stay were incubated with and without G-CSF (1, 10, 100 ng/ml). Reactive oxygen species (ROS) release and bactericidal activity against Staphylococcus aureus and Pseudomonas aeruginosa were evaluated. Plasma cytokines (interleukin 10, tumor necrosis factor α, and G-CSF) were measured. Results: Median values (25th-75th percentiles) indicated no stimulatory effect of G-CSF on neutrophil bactericidal activity against either organism: S. aureus, 100% (95-109) of the unstimulated condition with 1 ng/ml G-CSF, and P. aeruginosa, 102% (98-109) with 1 ng/ml G-CSF. However, wide inter-individual variability was found, ranging from marked inhibition to marked stimulation. Similar variability was found for ROS release. No correlations were found between ROS release and bactericidal activities against either bacterial strain. Inhibition of neutrophil bactericidal activity by G-CSF was associated with significantly higher plasma interleukin 10 concentrations. Plasma G-CSF levels were significantly higher in patients whose neutrophil bactericidal activity was unresponsive to G-CSF, suggesting G-CSF receptor downregulation. Conclusions: The effect of G-CSF on in vitro neutrophil bactericidal activity varied widely, depending on endogenous levels of G-CSF and was not predictable based on severity scores.
AB - Objective: Neutrophil function impairment is common in non-neutropenic critically ill patients. Whether granulocyte colony-stimulating factor (G-CSF) may be useful for preventing nosocomial infection in these patients is debated. The response of blood neutrophils from critically ill patients to G-CSF was investigated in vitro. Design and setting: Prospective study, laboratory investigation in two intensive care units. Patients: 52 critically ill patients without immunosuppression. Measurements: Neutrophils obtained from 52 patients on the 5th day of their intensive care unit stay were incubated with and without G-CSF (1, 10, 100 ng/ml). Reactive oxygen species (ROS) release and bactericidal activity against Staphylococcus aureus and Pseudomonas aeruginosa were evaluated. Plasma cytokines (interleukin 10, tumor necrosis factor α, and G-CSF) were measured. Results: Median values (25th-75th percentiles) indicated no stimulatory effect of G-CSF on neutrophil bactericidal activity against either organism: S. aureus, 100% (95-109) of the unstimulated condition with 1 ng/ml G-CSF, and P. aeruginosa, 102% (98-109) with 1 ng/ml G-CSF. However, wide inter-individual variability was found, ranging from marked inhibition to marked stimulation. Similar variability was found for ROS release. No correlations were found between ROS release and bactericidal activities against either bacterial strain. Inhibition of neutrophil bactericidal activity by G-CSF was associated with significantly higher plasma interleukin 10 concentrations. Plasma G-CSF levels were significantly higher in patients whose neutrophil bactericidal activity was unresponsive to G-CSF, suggesting G-CSF receptor downregulation. Conclusions: The effect of G-CSF on in vitro neutrophil bactericidal activity varied widely, depending on endogenous levels of G-CSF and was not predictable based on severity scores.
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U2 - 10.1007/s00134-002-1623-9
DO - 10.1007/s00134-002-1623-9
M3 - Article
C2 - 12541157
AN - SCOPUS:0037348607
SN - 0342-4642
VL - 29
SP - 396
EP - 402
JO - Intensive Care Medicine
JF - Intensive Care Medicine
IS - 3
ER -